Literature DB >> 2144945

Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome.

B Marino1, U Vairo, A Corno, S Nava, P Guccione, R Calabrò, C Marcelletti.   

Abstract

The atrioventricular canal is the "classic" congenital heart anomaly in Down syndrome. We may learn more of the nature of this disorder by careful study of the anatomic characteristics of the cardiac lesions and by comparing these lesions in patients with and patients without Down syndrome. We reviewed the clinical characteristics (echocardiographic and angiocardiographic) of 220 patients with atrioventricular canal and compared the prevalence of anatomic types and associated cardiac malformations in children with (105) and without (115) Down syndrome. In patients with Down syndrome, the complete form of atrioventricular canal was prevalent, with a high frequency of associated Fallot's tetralogy. Partial atrioventricular canal and left-sided anomalies were more common in patients without Down syndrome. Down syndrome is associated with a simpler type of atrioventricular canal when compared with patients with a normal chromosome configuration.

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Year:  1990        PMID: 2144945     DOI: 10.1001/archpedi.1990.02150340066025

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  26 in total

1.  Anterolateral muscle bundle of the left ventricle in atrioventricular septal defect: left ventricular outflow tract and subaortic stenosis.

Authors:  B Marino
Journal:  Pediatr Cardiol       Date:  1992-07       Impact factor: 1.655

2.  Isolated cleft of the mitral valve: its pathogenic relationship with endocardial cushion defects.

Authors:  Elena Boccuzzi; Emanuela Casinelli; Paolo Versacci; Bruno Marino
Journal:  Tex Heart Inst J       Date:  2010

Review 3.  Atrioventricular septal defect: from fetus to adult.

Authors:  Brian Craig
Journal:  Heart       Date:  2006-12       Impact factor: 5.994

4.  Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndrome.

Authors:  B Marino; M C Digilio; M G Gagliardi; A Giannotti; B Dallapiccola
Journal:  Pediatr Cardiol       Date:  1996 Jul-Aug       Impact factor: 1.655

5.  Morphogenetic alterations during endocardial cushion development in the trisomy 16 (Down syndrome) mouse.

Authors:  G G Hiltgen; R R Markwald; L L Litke
Journal:  Pediatr Cardiol       Date:  1996 Jan-Feb       Impact factor: 1.655

6.  A study to determine the prevalence of pulmonary arterial hypertension in children with Down syndrome and congenital heart disease.

Authors:  Mukti Sharma; Sanjeev Khera; Vishal Sondhi; Amit Devgan
Journal:  Med J Armed Forces India       Date:  2013-02-23

7.  Cardiac manifestations in a western moyamoya disease population: a single-center descriptive study and review.

Authors:  Anthony S Larson; Luis Savastano; James Klaas; Giuseppe Lanzino
Journal:  Neurosurg Rev       Date:  2020-06-07       Impact factor: 3.042

8.  Familial atrioventricular septal defect: possible genetic mechanism.

Authors:  M C Digilio; B Marino; A Giannotti; B Dallapiccola
Journal:  Br Heart J       Date:  1994-09

9.  Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal.

Authors:  M Gennarelli; G Novelli; M C Digilio; A Giannotti; B Marino; B Dallapiccola
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

10.  Atypical form of atrioventricular septal defect without left axis deviation: relation between morphology and unusual QRS axis.

Authors:  K Suzuki; Y Murakami; K Tatsuno; Y Takahashi; T Kikuchi; K Mori; S Mimori
Journal:  Br Heart J       Date:  1993-08
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